chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	29921565	29921579	TGTGTGTGTGTGTG	--------------	10	GENIC	possibly homozygous	50167711
12	29922441	29922443	TT	--	31	GENIC	possibly homozygous	50167713
12	29922449	29922451	TT	--	32	GENIC	possibly homozygous	50167715
12	29922466	29922467	T	TTG	24	GENIC	homozygous	50167717
12	29922532	29922533	C	T	53	GENIC	homozygous	50167719
12	29924236	29924237	A	G	47	GENIC	homozygous	50167721
12	29924339	29924340	A	G	59	GENIC	homozygous	50167723
12	29925303	29925304	C	G	50	GENIC	homozygous	50167725
12	29925701	29925702	C	G	56	GENIC	homozygous	50167727
12	29925853	29925854	G	A	47	GENIC	homozygous	50167729
12	29926237	29926238	A	-	23	GENIC	homozygous	50167731
12	29926301	29926302	C	T	23	GENIC	homozygous	50167733
12	29926639	29926640	T	TA	11	GENIC	heterozygous	50167735
12	29926652	29926653	C	-	23	GENIC	homozygous	50167737
12	29927227	29927228	G	GTT	38	GENIC	homozygous	50167739
12	29927475	29927476	T	-	31	GENIC	homozygous	50167741
12	29927654	29927655	C	T	30	GENIC	homozygous	50167743
12	29927794	29927795	A	T	27	GENIC	homozygous	50167745
12	29929329	29929330	C	T	44	GENIC	homozygous	50167747
12	29930337	29930338	A	G	41	GENIC	homozygous	50167749